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Folic Acid
Folic Acid - 0603-3714-32 - (Folic Acid)
Drug Information of Folic Acid
| Product NDC: | 0603-3714 |
| Proprietary Name: | Folic Acid |
| Non Proprietary Name: | Folic Acid |
| Active Ingredient(s): | 1 mg/1 & nbsp; Folic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Folic Acid
| Product NDC: | 0603-3714 |
| Labeler Name: | Qualitest |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080600 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19720331 |
Package Information of Folic Acid
| Package NDC: | 0603-3714-32 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0603-3714-32) |
NDC Information of Folic Acid
| NDC Code | 0603-3714-32 |
| Proprietary Name | Folic Acid |
| Package Description | 1000 TABLET in 1 BOTTLE (0603-3714-32) |
| Product NDC | 0603-3714 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Folic Acid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19720331 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest |
| Substance Name | FOLIC ACID |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
